美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
83008-020-08	83008-020	HUMAN PRESCRIPTION DRUG	Probenecid	Probenecid	TABLET, FILM COATED	ORAL	20230524	N/A	ANDA	ANDA080966	Quality Care Products, LLC	PROBENECID	500 mg/1	8 TABLET, FILM COATED in 1 BOTTLE (83008-020-08)
0527-1367-01	0527-1367	HUMAN PRESCRIPTION DRUG	Probenecid	Probenecid	TABLET, FILM COATED	ORAL	19760729	N/A	ANDA	ANDA080966	Lannett Company, Inc.	PROBENECID	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0527-1367-01)
0527-1367-10	0527-1367	HUMAN PRESCRIPTION DRUG	Probenecid	Probenecid	TABLET, FILM COATED	ORAL	19760729	N/A	ANDA	ANDA080966	Lannett Company, Inc.	PROBENECID	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (0527-1367-10)
71335-1697-1	71335-1697	HUMAN PRESCRIPTION DRUG	Probenecid	Probenecid	TABLET, FILM COATED	ORAL	20200825	N/A	ANDA	ANDA080966	Bryant Ranch Prepack	PROBENECID	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1697-1)
10135-541-01	10135-541	HUMAN PRESCRIPTION DRUG	Probenecid	Probenecid	TABLET, FILM COATED	ORAL	19760729	N/A	ANDA	ANDA080966	Marlex Pharmaceuticals Inc	PROBENECID	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-541-01)
10135-541-10	10135-541	HUMAN PRESCRIPTION DRUG	Probenecid	Probenecid	TABLET, FILM COATED	ORAL	19760729	N/A	ANDA	ANDA080966	Marlex Pharmaceuticals Inc	PROBENECID	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10)